Formulation of Self-Nanoemulsifying Drug Delivery System of Cephalexin: Physiochemical Characterization and Antibacterial Evaluation

A cephalexin (CEP) self-nanoemulsifying drug delivery system (SNEDDS) was developed in this study to improve the drug’s oral administration. The CEP-SNEDDS was made utilizing an aqueous titration method employing Lauroglycol 90, Poloxamer 188, and Transcutol-HP. Box-Behnken design (BBD) with three factors at three levels was used for optimization, and their impacts on globule size (nm), transmittance (percent), and emulsification time (s) were assessed. The optimized formulation (Opt-F3) was further tested for zeta potential, refractive index, percent transmittance, thermodynamic stability, in-vitro release, ex vivo permeability, antibacterial activity, and bioavailability. The chosen formulation (Opt-F3) had a globule size of 87.25 ± 3.16 nm, PDI of 0.25, zeta potential of −24.37 mV, self-emulsification duration of 52 ± 1.7 s, and percentage transmittance of 99.13 ± 1.5%, viscosity of 96.26 ± 2.72 cp, and refractive index of 1.29 ± 0.1. It showed a sustained release profile (94.28 ± 5.92 percent in 24 h). The Opt-F3 formulation had 3.95 times the permeability of CEP-dispersion. In comparison to CEP-dispersion, it also demonstrated greater antibacterial efficacy against tested Gram-positive and Gram-negative pathogens. The oral bioavailability of Opt-F3 is 3.48 times higher than that of CEP-dispersion, according to an in-vivo investigation. It has been determined that the prepared CEP-SNEDDS may be an advantageous carrier for CEP delivery.


Introduction
Cephalexin (CEP) is a first-generation cephalosporin derivative that is given orally. It belongs to the β-lactam class of antibiotics and is commercially available as a monohydrate. It has chemical formula C 16 H 17 N 3 O 4 S·H 2 O and a molecular weight of 365.41 g/mol [1]. It is effective in the treatment of Staphylococci and Streptococci infections [2]. It was also found to be effective against Escherichia coli [3]. It is listed as a key access antibiotic in PEG200 and HCl were acquired from Acros Organics (Mumbai, India). Poloxamer188 and other chemicals were obtained from Sigma Aldrich (St-Louis, MO, USA).

Preliminary Screening
The equilibrium solubility method was used to select the oil, surfactant, and cosurfactant [22]. The solubility of CEP in each components was evaluated in order to select the oil, surfactant, and co-surfactant. The screening was performed in variety of oils, surfactants, and co-surfactants. In a clean glass vial, 1.5 mL of each oil, surfactant, and co-surfactant was added, along with an excess of CEP. The vials were capped properly and shaken on a mechanical shaker at 37 ± 0.5 • C for 72 h. The samples were centrifuged at 10,000 rpm for 5 min and then supernatant was collected. The amount of CEP dissolved in each component was analyzed at 262 nm with the help of UV spectrophotometer (Shimadzu 1800, Kyoto, Japan) after a suitable dilution.

Pseudo Ternary Diagram
The purpose of making a pseudo ternary diagram was to choose emulsification efficiency and a reasonable oil, surfactant, and co-surfactant concentration [23]. This was achieved using the aqueous titration method. To prepare variable ratios, a combination of surfactant and co-surfactant was used (1:0, 1:1, 1:2, 2:1, 1:3). Smix was mixed with oil in various ratios ranging from 9:1 to 1:9, and then titrated with a predetermined amount of double-distilled water. The presence of turbidity was carefully inspected visually after the complete reaction. Using a phase diagram, the self-nanoemulsifying zone was calculated (triangular co-ordinate software). The ratio of oil, surfactant, and co-surfactant was calculated using the maximum area. The three levels of each component were selected for further investigation (Table 1). Table 1. Formulation variables and their responses used to optimize CEP SNEDDS.

Optimization
Box Behnken design (BBD, DoE Software, Stat-Ease, Minneapolis, MN, USA) was used to analyze the effect of independent constraints (oil, surfactant and co-surfactant) on the different dependent responses (globule size, % transmittance, emulsification time). It works on the principle of response surface methodology and gives fewer compositions than a parallel response surface design (central composite design). It revealed the effect of formulation constraints individually, their interactions, and quadratic expressions [24]. The three factors at three levels, depicted a total of seventeen runs with five similar compositions to assess the error. The data was applied to various models, viz linear, 2F1, and quadratic to explore the influence of independent variables. ANOVA, polynomial equations, and surface plots were generated and explored the effect of independent variables on the dependent variables.

Preparation of CEP-Loaded SNEDDS
The aqueous titration method was used for preparation of CEP-SNEDDS [22]. A total of seventeen formulations were developed as per the composition given in Table 2. Oil (A), surfactant (B), and co-surfactant (C) were chosen and mixed in a glass vial to form a homogenous mixture (F1-F17). The samples (F1-F17) were vortexed with CEP (100 mg) to obtain a uniform homogenous mixture. The formulations were stored at room temperature for further characterization [25].

Evaluation of CEP SNEDDS Droplet Characterization
The particle size analyzer (ZEN-3600, Malvern, Malvern Instruments, Westborough, MA 01581, USA) was used to evaluate droplet size, polydispersibility index and zeta potential. CEP-SNEDDS were diluted (100-fold) with deionized water and transferred to a cuvette for evaluation. The surface morphology was evaluated by transmission electron microscopy (TEM, Mic JEM1011, JEOL, Tokyo, Japan). A drop of CEP-SNEDDs was placed on a carbon-coated copper grid and kept for a few minutes. Then phosphotungistic acid as staining agent was added to the sample. Any excess was removed with filter paper and the sample was air-dried. The grid was placed in the TEM instrument and the image was captured. Detection of Self-Nanoemulsification Time Self-emulsification time is the time required for the sample to become self-emulsified with distilled water. The self-emulsification process was visually evaluated for the emulsification property [22]. The study was performed with a USP paddle-type apparatus (Sotex AG, Aesch, Switzerland) to determine the emulsification time. Distilled water (500 mL) was placed in the vessel, and the temperature and rotation speed were set at 37 ± 0.5 • C and 50 rpm, respectively. CEP-SNEDDS was added to the media and then the emulsification time was noted.
Percentage Transmittance CEP-SNEDDS was diluted 100-fold with distilled water and the percentage transmittance was determined by UV visible spectrophotometer at 638 nm. The study was performed in triplicate for each formulation. The stability of CEP-SNEDD (Opt-F3) was evaluated by applying various stressors, i.e., centrifugation, heating cooling and freeze-thawing.
Heating and cooling study: This study was performed by taking Opt-F3 and kept at 4-40 • C for 48 h. Then the samples were assessed for instability (phase separation, creaming and phase inversion).
Freeze-thaw stability: Reconstituted optimized SNEDDS (Opt-F3) was kept under temperature range of −20 to 25 • C for 48 h and examined visually for any instability.

DSC Analysis
DSC analysis was performed for CEP, Lauroglycol 90, Poloxamer 188, Transcutol HP, and optimized SNEDDS (Opt-F3) using a DSC instrument (Mettler Toledo, Toledo, OH, USA). In brief, about 5 mg of each sample was packed into an aluminum pan and placed into the DSC instrument. The samples were examined between 20-450 • C at a heating rate of 10 • C/min with a continuous supply of nitrogen at 50 mL/min. An empty aluminum pan was used as a reference. The thermogram was collected to interpret the changes in sample behaviour.

Drug Release Study
The study of CEP from Opt-F3 was studied in a USP paddle dissolution apparatus. The release medium (0.1 N HCl, pH-1.2, 900 mL) was placed into a basket and maintained at 37 ± 0.5 • C to simulate stomach condition. The sample was placed in a dialysis bag (MW CO-12 kDa) and tied from both ends. The dialysis bag was attached to a paddle, dipped into a dissolution medium and rotated at 100 rpm. At a predetermined time, 5 mL of the sample was withdrawn, suitably diluted and filtered. The absorbance was analyzed by UV visible spectrophotometer at 262 nm [6,27]. The release was calculated and a graph between % drug release and time was plotted. A similar study was performed for pure CEP in similar condition for comparison. The release data fitted to various kinetic models to evaluate the release kinetics and release mechanism [24,28].

Ex-Vivo Permeation Study
The study was performed using goat intestine collected from a slaughterhouse. The intestine was cleaned in a biological Ringer solution and filled with the formulation. The intestine was tied at both ends and dipped in biological Ringer solution (100 mL). The study was conducted on a magnetic stirrer (50 rpm) and the temperature was maintained at 37 ± 0.5 • C. At a predetermined time, 2 mL sample was taken up to 6 h and drug permeation was analyzed [6,29], using UV visible spectrophotometry at 262 nm. The same procedure was repeated with pure CEP-dispersion in water. A graph of the amount of drug permeated versus time was plotted. The different parameters i.e., flux (J, µg/cm 2 /h), permeability coefficient (PC) and enhancement ratio (ER) were calculated using the following equations [27,30]: The antimicrobial study was conducted on S. aureus (Gram positive,) and E. coli (Gram negative). The study was performed by the diffusion method [31]. The efficacy was determined in the terms of zone of inhibition (ZOI) and findings were compared between opt-F3 and pure CEP-dispersion. The test organisms were grown on sterile Luria Bertani broth and the plates were cultured with 100 µL of bacteria. Ten mL of nutrient agar were transferred to the plates and allowed to solidify. Three wells were made on each plate and sample (100 µL) was placed to each well. The plates were incubated for 48-72 h in an incubator set at 37 ± 0.5 • C [19,32]. Each experiment was conducted in triplicate and the zone of inhibition was then measured.

Bioavailability Study
The study was performed in albino Wistar rats (200-250 gm of either sex). The animal study protocol was approved by the Institutional Animal Ethical Committee of the Hygia Institute of Pharmaceutical Education and Research (Lucknow, India; IAEC No. HIPER/IAEC/69/21/04). Rats were obtained from the animal house and kept under the recommended conditions with free access to food and water. Before the experiment, the animals were allowed to acclimatize to normal conditions (25 ± 2 • C, and 12 h day/night cycle) for a week. The rats were divided into two groups, where Group I received pure CEP dispersion and Group II received the optimized SNEDDS (Opt-F3) (equivalent to 22 mg/kg of CEP) orally. The dose was calculated based on the body surface area in comparison to humans. After oral administration, blood samples were withdrawn from the retro-orbital plexus into a pre-heparinized tube at different time points (0, 0.5, 1, 2, 4, 6, and 12 h). The blood was centrifuged at 4000 rpm for 15 min (Remi Centrifuge, Mumbai, India) and the plasma separated.

Extraction of CEP from Plasma
In a tube, the plasma sample (0.2 mL) was combined with perchloric acid for deproteination (0.2 mL, 70%) and vortexing (2 min). Finally, the sample was centrifuged for 10 min at 12,000 rpm, and the supernatant recovered. The extract was dissolved in methanol after the supernatant was dried under vacuum. HPLC (LC 10 AD model, Shimadzu, Tokyo, Japan) was used for the analysis. The instrument was connected to a gradient flow pump that included an auto sampler and C 18 column (D150 × 4.6 mm, 5 µm). The sample (20 µL) was injected into the column and 0.01 mol/L sodium acetate buffer/methanol (25:75, v/v) was used as mobile phase with a flow rate of 1 mL/min. detection was carried out with a UV-detector set at 262 nm.

Pharmacokinetic Study
For the above said method, plasma drug concentration at various times was obtained. A plot of plasma concentration vs. time was constructed and different pharmacokinetic parameters Cmax, Tmax, AUC, half-life (t 1/2 ), elimination rate constant (Kel) etc. were calculated. Finally, the relative bioavailability was determined in comparison to CEP dispersion:

Statistical Analysis
All results were expressed in the terms of mean ± SD. GraphPad Prism (GraphPad Software, San Diego, CA 92108, USA) was used for statistical analysis. For the comparison analysis, Student's-test and analysis of variance (ANOVA) with Tukey Karman post-test was applied. Figure 1A-C shows the solubility of CEP in different oils, surfactants, and co-surfactants, and selection was made based on the highest solubility. Lauroglycol l90 > Caprol PGE-860 > eucalyptus oil > almond oil > sunflower oil is the order of CEP solubility in different oils ( Figure 1A). Poloxamer188 > Solutol HS 15 > Tween 20 > Cremophor RH 40 > Span 20 and Transcutol HP > PEG400 > PEG200 > PG is the order of CEP solubility in surfactant and co-surfactant ( Figure 1B,C). Lauroglycol 90 (61.37 ± 3.72 mg/mL), Poloxamer 188 (85.26 ± 6.28 mg/mL), and Transcutol HP (120.32 ± 9.36 mg/mL) as oil, surfactant, and co-surfactant, respectively. Poloxamer 188 is a surfactant that is hydrophilic and has an HLB value of 29. It allows SNEDDS to quickly emulsify when they come into contact with water.

Statistical Analysis
All results were expressed in the terms of mean ± SD. GraphPad Prism (GraphPad Software, San Diego, CA 92108, USA) was used for statistical analysis. For the comparison analysis, Student's-test and analysis of variance (ANOVA) with Tukey Karman post-test was applied. Figure 1A-C shows the solubility of CEP in different oils, surfactants, and co-surfactants, and selection was made based on the highest solubility. Lauroglycol l90 > Caprol PGE-860 > eucalyptus oil > almond oil > sunflower oil is the order of CEP solubility in different oils (Fig. 1A). Poloxamer188 > Solutol HS 15 > Tween 20 > Cremophor RH 40 > Span 20 and Transcutol HP > PEG400 > PEG200 > PG is the order of CEP solubility in surfactant and co-surfactant ( Fig. 1B-C). Lauroglycol 90 (61.37 ± 3.72 mg/mL), Poloxamer 188 (85.26 ± 6.28 mg/mL), and Transcutol HP (120.32 ± 9.36 mg/mL) as oil, surfactant, and co-surfactant, respectively. Poloxamer 188 is a surfactant that is hydrophilic and has an HLB value of 29. It allows SNEDDS to quickly emulsify when they come into contact with water.

Preparation of the Pseudo Ternary Diagram
The goal of constructing the phase solubility diagram was to get a large enough self-emulsification zone [15,33]. To obtain a clear and stable SNEDDS, multiple surfactant and co-surfactant ratios (1:1, 1:2, 2:1) were examined, as well as varied oil ratios (9:1, 1:9), as shown in Figure 2. The best surfactant and co-surfactant ratio (Smix) was discovered to be 2:1, which demonstrated a clear zone when compared to the other surfactant and co-surfactant ratios of 1:1 and 1:2. The absorption of surfactant at the oil-water interface, which is responsible for the lowering of interfacial tension, could explain the transparency of the zone in the Smix 2:1 ratio [15,34], so from the phase diagram, oil (Lauroglycol 90, 5-28%, w/w), surfactant (Poloxamer 188, 32-78%, w/w) and co-surfactant (Transcutol HP, 8-52%, w/w) was used for the optimization and preparation of SNEDDS.
shown in Figure 2. The best surfactant and co-surfactant ratio (Smix) was discovered to be 2:1, which demonstrated a clear zone when compared to the other surfactant and cosurfactant ratios of 1:1 and 1:2. The absorption of surfactant at the oil-water interface, which is responsible for the lowering of interfacial tension, could explain the transparency of the zone in the Smix 2:1 ratio [15,34], so from the phase diagram, oil (Lauroglycol 90, 5-28%, w/w), surfactant (Poloxamer 188, 32-78%, w/w) and co-surfactant (Transcutol HP, 8-52%, w/w) was used for the optimization and preparation of SNEDDS.

Optimization
To find the best composition, three independent variables were used: oil (Lauroglycol 90, 5-28%), surfactant (Poloxamer 188, 32-78%), and co-surfactant (Transcutol HP, 8-52%. This data was fed into the optimization model, yielding 17 different compositions, including five common formulas (center point). The data was fitted to various models, and the quadratic model proved to be best fit as seen in Table 3.

Optimization
To find the best composition, three independent variables were used: oil (Lauroglycol 90, 5-28%), surfactant (Poloxamer 188, 32-78%), and co-surfactant (Transcutol HP, 8-52%. This data was fed into the optimization model, yielding 17 different compositions, including five common formulas (center point). The data was fitted to various models, and the quadratic model proved to be best fit as seen in Table 3. As presented in Table 2, globule size (Y 1 ) of CEP-SNEDDs (F1-F17) was found to be in the range of 30.66-205.84 nm. The data was added to the design and the polynomial Equation (5) was generated, as shown below: Globule size (Y 1 , nm) = +108.99 + 57.79A − 28.91B − 222.44C − 11.73AB + 0.81AC − 5.448BC − 4.03A 2 + 5.24B 2 + 5.04C 2 It may be inferred from the above equation that model term A had a positive effect on the size, but model terms B and C had a negative effect. The model terms A, B, C, AB, BC, A 2 , B 2 , and C 2 were all found to be significant (p < 0.05), but AC was found to be non-significant (p > 0.05). The "Pred R-Squared (0.9885)" and "Adj R-Squared (0.9957)" were found to be in reasonable agreement. The quadratic model, as indicated in Table 3, was the best-fitting model. The first variable oil (A) had a positive effect on globule size, while the second variable surfactant (B) and the third variable co-surfactant (C) had a negative effect. The size of globules increases as oil content rises. Due to partial emulsification in the presence of insufficient surfactant and co-surfactant concentrations, the size of the globules increased (F1-F2) as the oil concentration increased (F1-F2). On other hand, as concentration of surfactant and co-surfactant increases, the size of the globules decreased (F1-F3 and F6-F8). This could be due to surfactant and co-surfactant accessibility at the oil/water interface, which helped to reduce interfacial tension and contribute to system stability [16,18]. Similar findings have already been reported in literature [22,23]. The surfactant and co-surfactant together showed opposite effect, with globule size decreasing as the concentration increased. This could be due to the significant effect of either surfactant or co-surfactant on globule size, as both had the same effect. When both oil and surfactant are increased, globule size falls due to surfactant's dominant influence over the oil. However, increasing the oil and co-surfactant concentrations together increases the viscosity of the medium due to the dominant influence of oil over the co-surfactant. The 3D graphics show the effect of all independent factors on globule size, including oil, surfactant, and co-surfactant ( Figure 3A).

Effect of Variables on Transmittance (Y 2 , %)
The transmittance (%, Y 2 ) for all developed CEP-SNEDDS was found to be in the range of 83.73 (F2)-99.39% (F7) as shown in Table 2. A polynomial equation (Equation (6)) was used to interpret effect of independent variables on the transmittance (%).
Transmittance (Y 2 , %) = +96.29 − 4.79 A + 3.88B + 2.50C + 2.95 AB − 1.28 AC + 0.81BC − 2.39 A 2 − 1.24B 2 − 2.19 C 2 (6) It may be inferred from the above equation that the term A has a negative impact, and the terms B as well as C, had a favorable effect on the transmittance (%, Y 2 ). The transmittance (%) decreased as the oil content increased (F1-F2). This could be caused by an insufficient amount of surfactant and co-surfactant [29,33]. On the other hand, when the concentration of surfactant and co-surfactant increases, the transmittance also increases (F1-F3 and F6-F8). This could be due to surfactant and co-surfactant accessibility at the oil/water interface, which helped to reduce interfacial tension and increase transmittance. A similar finding was reported for an atorvastatin calcium SNEDDS [23]. The combined impact also revealed that when the concentration of oil (A) and surfactant (B) rises, the transmittance is also increased. As a result, as oil and co-surfactant concentrations increase, the transmittance (percent) rises. This could be attributed to liquid crystal formation as well as an increase in the system's viscosity. 3D images shows effect of all independent factors on transmittance, including oil (A), surfactant (B), and co-surfactant (C) ( Figure 3B). All terms A, B, C, AB, AC, BC, A 2 , B 2 , and C 2 were considered to be important in this case. The "Pred R-Squared (0.9988)" and "Adj R-Squared (0.9995)" were found to be in reasonable agreement. Table 3 shows the statistical summary of the best-fitted model, which was found to be a quadratic one.

Effect of Variables on Transmittance (Y2, %)
The transmittance (%, Y2) for all developed CEP-SNEDDS was found to be in the range of 83.73 (F2)-99.39% (F7) as shown in Table 2. A polynomial equation (Equation (6)) was used to interpret effect of independent variables on the transmittance (%).
It may be inferred from the above equation that the term A has a negative impact, and the terms B as well as C, had a favorable effect on the transmittance (%, Y2). The transmittance (%) decreased as the oil content increased (F1-F2). This could be caused by an insufficient amount of surfactant and co-surfactant [29,33]. On the other hand, when the concentration of surfactant and co-surfactant increases, the transmittance also increases (F1-F3 and F6-F8). This could be due to surfactant and co-surfactant accessibility at the oil/water interface, which helped to reduce interfacial tension and increase transmittance. A similar finding was reported for an atorvastatin calcium SNEDDS [23]. The combined impact also revealed that when the concentration of oil (A) and surfactant (B) rises, the transmittance is also increased. As a result, as oil and co-surfactant concentrations in-

Effect of Variables on Emulsification Time (Y 3 , s)
The emulsification time of prepared CEP-SNEDDs was found to be in range 25 s (F12)-146 s (F2) ( Table 2). The data fed were the actual data of emulsification time (Y 3 , s) and the following Equation (7) F3 and F6-F8). This could be due to surfactant and co-surfactant accessibility at oil/water interface, which reduces interfacial tension and hence reduces emulsification time. Similar findings have already been reported in the literature [23,35]. Due to the dominant effect of surfactant, the emulsification time reduced as the oil (A) and surfactant (B) were increased. The 3D images illustrate the effect of all independent factors on transmittance, including oil, surfactant, and co-surfactant ( Figure 3C). The significant model terms in this situation were A, B, C, AB, AC, BC, A 2 , B 2 , C 2 . The "Pred R-Squared (0.9968)" and "Adj R-Squared (0.9992)" were found to be in reasonable agreement. Table 3 tabulates analysis data for quadratic model, which was shown to be best-fitted model.

Point Prediction for Optimization
For the point prediction, we used Formula F13 from Table 2. Further adjustments in composition were made in a point prediction, and their effects on globule size (nm), transmittance (percent), and emulsification time were recorded (s). Table 4 shows the alterations that were made in the composition with their findings. With oil at 14%, surfactant at 59%, and co-surfactant at 32%, the formulation opt-F3 was chosen as the best. Predicted value of globule size, transmittance, and emulsification time were found to be 84.39 nm, 98.84%, and 49.44 s, respectively. The experimental values of globule size, transmittance, and emulsification time was found to be 87.25 ± 3.16 nm, 99.13 ± 0.5 percent, and 52 ± 1.7 s, respectively. The results revealed that the percent variation between the actual and experimental values was quite low, indicating that model was well fitted.

Droplet Characterization
The globule size, PDI and zeta potential for the optimized formulation (Opt-F3) were found to be 87.25 ± 3.16 ( Figure 4A), 0.25, and −24.37 mV, respectively. The low PDI value (<0.5) indicates desired stability of Opt-F3. TEM images showed spherical shaped globules with a uniform surface ( Figure 4B).

Droplet Characterization
The globule size, PDI and zeta potential for the optimized formulation (Opt-F3) were found to be 87.25 ± 3.16 ( Figure 4A), 0.25, and −24.37 mV, respectively. The low PDI value (<0.5) indicates desired stability of Opt-F3. TEM images showed spherical shaped globules with a uniform surface ( Figure 4B).

Characterization of Optimized SNEDDS (Opt-F3)
The CEP-SNEDDS-opt was subjected to a variety of stressful conditions, including centrifugation, heating, cooling, and a freeze-thaw cycle, among others (Opt-F3). Even after the induction of stress conditions, the formulation was found to be physically stable following emulsification, with no indications of instability such as creaming, cracking, or phase separation. At 25 ± 2 °C, the improved formulation (Opt-F3) had a viscosity of 96.26

Characterization of Optimized SNEDDS (Opt-F3)
The CEP-SNEDDS-opt was subjected to a variety of stressful conditions, including centrifugation, heating, cooling, and a freeze-thaw cycle, among others (Opt-F3). Even after the induction of stress conditions, the formulation was found to be physically stable following emulsification, with no indications of instability such as creaming, cracking, or phase separation. At 25 ± 2 • C, the improved formulation (Opt-F3) had a viscosity of 96.26 ± 2.72 cps and a refractive index of 1.29 ± 0.17.

DSC Analysis
The thermograms in Figure 5A-E show the results of our DSC investigation of pure CEP, CEP-SNEDDS-opt, and the utilized components. The crystalline character of CEP was demonstrated by a strong peak at 319.24 • C ( Figure 5A). The thermodynamic peak for Poloxamer was observed at 57.37 • C, whereas a wide peak for Lauroglycol 90 was seen at 329.57 • C ( Figure 5B,C). At 140 • C and 210 • C, Transcutol HP showed minor peaks ( Figure 5D). The CEP peak was not visible in the Opt-F3 formulation ( Figure 5E). Opt-F3's thermogram, on the other hand, showed fewer strong peaks. The complete solubilization of the drug in SNEDDS components was revealed by the lack of a prominent endothermic peak of CEP in SNEDDS [36,37].

In-Vitro Drug Release
The release study of Opt-F3 and pure CEP dispersion was carried out, and the results are plotted in Figure 6. Opt-F3 demonstrated a rapid release of 21.47 ± 3.83 % CEP in the first 2 h, followed by a protracted release of 94.28 ± 5.92 % in 24 h. The presence of CEP on the surface of SNEDDS could explain the initial rapid release. The entrapped drug within SNEDDS, on the other hand, allowed for longer-lasting drug release. In the same period, the drug release from CEP dispersion was determined to be very low at 26.76 ± 3.28 %. It could be due to CEP's low solubility. The release data of the Opt-F3 formulation was submitted to various kinetic models, with a first-order one proving the best fit (R 2 = 0.9815). A non-Fickian transport kind of release mechanism was demonstrated by the release ex-

In-Vitro Drug Release
The release study of Opt-F3 and pure CEP dispersion was carried out, and the results are plotted in Figure 6. Opt-F3 demonstrated a rapid release of 21.47 ± 3.83% CEP in the first 2 h, followed by a protracted release of 94.28 ± 5.92% in 24 h. The presence of CEP on the surface of SNEDDS could explain the initial rapid release. The entrapped drug within SNEDDS, on the other hand, allowed for longer-lasting drug release. In the same period, the drug release from CEP dispersion was determined to be very low at 26.76 ± 3.28%. It could be due to CEP's low solubility. The release data of the Opt-F3 formulation was submitted to various kinetic models, with a first-order one proving the best fit (R 2 = 0.9815). A non-Fickian transport kind of release mechanism was demonstrated by the release exponent of n = 0.7128.

Ex-Vivo Permeation Study
The amount of CEP released from Opt-F3 was considerably (p < 0.01) larger than that of CEP-dispersion, according to the permeation study results. The Opt-F3 formulation flux (J) was determined to be 11.24 ± 2.41 μg/cm 2 /h, which is larger than CEP-dispersion flux (2.84 ± 0.35 μg/cm 2 /h). For the Opt-F3 formulation and CEP-dispersion, the permeability coefficients (PC) were found to be 0.022 cm/s and 0.0057 cm/s, respectively. The ER ratio was also calculated, and the results revealed that Opt-F3 had a flux that was 3.95 times higher than that of CEP-dispersion. These results were made possible by the presence of surfactants and co-surfactants, which are responsible for solubility of poorly soluble drugs as well as the opening of the intestinal membrane's tight junction.

Antimicrobial Study
To test the effectiveness of Opt-F3 and CEP-dispersion, antibacterial activity was performed against S. aureus and E. coli bacteria and results shown in Figure 7. The zone of inhibition (ZOI) of the Opt-F3 formulation was 15.27 ± 1.52 mm against S. aureus and 10.83 ± 1.37 mm against E. coli. Against E. coli and S. aureus administration of CEP-dispersion resulted in a significant (P0.05) change in ZOI, with a ZOI of 7.39 ± 1.23 against S. aureus and 5.13 ± 0.98 against E. coli being found. According to the findings, the produced SNEDDS had enhanced activity due to the better solubility of CEP in the presence of oil, surfactant, and co-surfactant. Because of the nano-droplet size and increased solubility of CEP, the SNEDDS have greater activity. The larger effective surface area available for drug absorption is due to the nanosize range. It also resulted in increased CEP solubility and a higher amount of medication on the target side to trigger the effect. CEP works by breaking down the microorganisms' cell walls. Internalization of the medication in the cell wall of the microorganism occurs, resulting in cell lysis via blocking the interaction between N-acetylmuramic acid and N-acetylglucosamine [38,39].

Ex-Vivo Permeation Study
The amount of CEP released from Opt-F3 was considerably (p < 0.01) larger than that of CEP-dispersion, according to the permeation study results. The Opt-F3 formulation flux (J) was determined to be 11.24 ± 2.41 µg/cm 2 /h, which is larger than CEP-dispersion flux (2.84 ± 0.35 µg/cm 2 /h). For the Opt-F3 formulation and CEP-dispersion, the permeability coefficients (PC) were found to be 0.022 cm/s and 0.0057 cm/s, respectively. The ER ratio was also calculated, and the results revealed that Opt-F3 had a flux that was 3.95 times higher than that of CEP-dispersion. These results were made possible by the presence of surfactants and co-surfactants, which are responsible for solubility of poorly soluble drugs as well as the opening of the intestinal membrane's tight junction.

Antimicrobial Study
To test the effectiveness of Opt-F3 and CEP-dispersion, antibacterial activity was performed against S. aureus and E. coli bacteria and results shown in Figure 7. The zone of inhibition (ZOI) of the Opt-F3 formulation was 15.27 ± 1.52 mm against S. aureus and 10.83 ± 1.37 mm against E. coli. Against E. coli and S. aureus administration of CEP-dispersion resulted in a significant (P0.05) change in ZOI, with a ZOI of 7.39 ± 1.23 against S. aureus and 5.13 ± 0.98 against E. coli being found. According to the findings, the produced SNEDDS had enhanced activity due to the better solubility of CEP in the presence of oil, surfactant, and co-surfactant. Because of the nano-droplet size and increased solubility of CEP, the SNEDDS have greater activity. The larger effective surface area available for drug absorption is due to the nanosize range. It also resulted in increased CEP solubility and a higher amount of medication on the target side to trigger the effect. CEP works by breaking down the microorganisms' cell walls. Internalization of the medication in the cell wall of the microorganism occurs, resulting in cell lysis via blocking the interaction between N-acetylmuramic acid and N-acetylglucosamine [38,39].

Bioavailability Study
A pharmacokinetic investigation was carried out on albino Wistar rats following a single oral dose of SNEDDS-opt (Opt-F3) and CEP-dispersion, with the results presented in Table 5. The Cmax of the formulation Opt-F3 was 7.68 ± 0.72 g/mL, which was significantly greater (p < 0.05) than that of CEP-dispersion (4.68 ± 0.57 g/mL). Tmax was likewise found to be higher (4 h) than that of CEP-dispersion (2 h), indicating that CEP was released continuously from SNEDDS. Because of the sustained CEP release from SNEDDS, the half-life (t1/2) was observed to be substantially (p < 0.05, 5.9 h) longer than with CEP-dispersion (1.4 h). The AUC0-t and AUC0-∞ values were determined to be 71.37 ± 4.28 g.h/mL and 77.31 ± 4.87 g.h/mL, respectively, which were considerably (p < 0.05) higher than the CEP-dispersion values of 20.5 ± 3.76 g.h/mL and 20.73 ± 3.76 g.h/mL. Opt-F3 has an elimination rate constant (Kel) of 0.12 h −1 , which is significantly (p < 0.05) lower than that of CEP-dispersion. Opt-F3 had a 3.48-fold better percent bioavailability than CEP-dispersion. This suggested that the SNEDDS formulation could be a viable option for improving CEP oral bioavailability. Table 5. Pharmacokinetic parameters of CEP-SNEDDS (Opt-F3) and CEP dispersion after singledose oral administration. The study performed with six rats in each group and data given as mean± SD.

Bioavailability Study
A pharmacokinetic investigation was carried out on albino Wistar rats following a single oral dose of SNEDDS-opt (Opt-F3) and CEP-dispersion, with the results presented in Table 5. The Cmax of the formulation Opt-F3 was 7.68 ± 0.72 g/mL, which was significantly greater (p < 0.05) than that of CEP-dispersion (4.68 ± 0.57 g/mL). Tmax was likewise found to be higher (4 h) than that of CEP-dispersion (2 h), indicating that CEP was released continuously from SNEDDS. Because of the sustained CEP release from SNEDDS, the halflife (t 1/2 ) was observed to be substantially (p < 0.05, 5.9 h) longer than with CEP-dispersion (1.4 h). The AUC 0-t and AUC 0-∞ values were determined to be 71.37 ± 4.28 g·h/mL and 77.31 ± 4.87 g·h/mL, respectively, which were considerably (p < 0.05) higher than the CEP-dispersion values of 20.5 ± 3.76 g·h/mL and 20.73 ± 3.76 g·h/mL. Opt-F3 has an elimination rate constant (Kel) of 0.12 h −1 , which is significantly (p < 0.05) lower than that of CEP-dispersion. Opt-F3 had a 3.48-fold better percent bioavailability than CEP-dispersion. This suggested that the SNEDDS formulation could be a viable option for improving CEP oral bioavailability. Table 5. Pharmacokinetic parameters of CEP-SNEDDS (Opt-F3) and CEP dispersion after single-dose oral administration. The study performed with six rats in each group and data given as mean ± SD.

Conclusions
CEP-loaded SNEDDS for oral delivery of the drug was developed successfully. The formulation exhibited acceptable globule size, high transmittance, and short self-emulsification time. The in-vitro drug release for the optimized formulation (Opt-F3) was significantly higher than that of pure drug (CEP) dispersion. Moreover, the optimized formulation exhibited three times better permeation than that of CEP dispersion. The formulation Opt-F3 exhibited a greater antimicrobial potential in comparison to pure CEP-dispersion. The in-vivo study indicated that the oral bioavailability of developed formulation was 3.48-fold higher than that of CEP-dispersion. SNEDDS displayed the desired stability under the stated conditions studied. Finally, it could be concluded that the developed CEP-SNEDDS was proved to be a promising carrier for CEP delivery in the treatment of microbial disorders.

Data Availability Statement:
The data presented in this study are available on request from the corresponding author.